Senior Clinical Research Scientist

Healthcare Professionals Group; Sydney; On-site; AUD 90,000 - 120,000; Full time

Job summary

A leading recruitment firm in healthcare is seeking a Senior Clinical Research Scientist to lead the design and execution of clinical studies. You will work with medical experts to generate clinical evidence for next-generation health technologies. Ideal candidates have a degree in life sciences and at least 5 years of clinical research experience, particularly in a product development setting for medical devices.

Qualifications

• Minimum 5 years of experience in clinical research, specifically in medical devices.
• Proven track record of designing and executing clinical studies.
• Knowledge of infection prevention and/or microbiology is essential.

Responsibilities

• Develop clinical study protocols based on regulatory standards.
• Oversee study conduct, including design and monitoring.
• Collaborate with teams to incorporate clinical evidence into product development.

Skills

Project management

Problem-solving

Communication

Interpersonal abilities

Education

Degree in a life sciences discipline

Job description

1 day ago Be among the first 25 applicants

Direct message the job poster from Healthcare Professionals Group

Senior Recruitment Consultant - Life Science | Medical Affairs | Regulatory Affairs | Clinical Research | Quality Assurance at Healthcare…

Senior Clinical Research Scientist

• Centre of the Action Designing & Leading Trials from Scratch
• Drive Clinical Innovation & Shape Global Health Tech
• Endless Career Opportunities and Development

This is a rare opportunity for a Senior Clinical Research Scientist to take full scientific ownership and deliver real-world impact. You’ll lead the design and execution of clinical studies across both new product innovations and exploratory research areas across medical devices.


Joining a lean, agile team, you’ll partner with top-tier medical experts to generate the clinical evidence behind next generation health technologies.


This is once in a lifetime opportunity to step into a fast-growing international company at the forefront of medical innovation, committed to improving patient outcomes and raising the standard of care.



Duties

• Develop clinical study protocols based on regulatory standards/guidelines and literature and contribute to publication strategy

• Oversee all aspects of study conduct, including study design, protocol development, statistical approach, development of study procedures, data collection, and monitoring
• Analyse study data and prepare comprehensive reports summarizing findings
• Collaborate with cross-functional teams to incorporate clinical evidence into product development

Skills and Experience

• Degree in a life sciences discipline and knowledge of infection prevention and/or microbiology
• Minimum 5 years of experience in clinical research, in a product development setting for medical devices
• Proven track record of successfully designing and executing clinical studies, including protocol writing
• Understanding of laboratory procedures and equipment
• Excellent project management and problem-solving skills
• Strong communication and interpersonal abilities to effectively liaise with internal and external stakeholders

Culture
Our client values innovation, collaboration, and a commitment to excellence. They offer a supportive, inclusive work environment that encourages professional growth and recognizes individual contributions.



If you’re interested in discussing this role, please contact Eve Cooke at HPG on [phone] or email me your CV at [e-mail]

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

• Industries

  Medical Equipment Manufacturing

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